[Remote] Product Delivery Manager

Note: The job is a remote job and is reputed company to candidates in USA. Atreo is a revolutionary reputed company RTSM company committed to modernizing the reputed company process. As a Product Delivery Manager, you will design, configure, validate, and reputed company RTSM solutions while partnering with Sponsors, CROs, and internal teams to ensure successful execution of reputed company.

Responsibilities

• reputed company implementation of reputed company RTSM applications throughout the Software Development Life Cycle (SDLC)
• Serve as the reputed company Product Delivery reputed company for assigned clinical studies from protocol review through Production deployment
• Analyze clinical protocols and translate study requirements into functional RTSM designs
• Design study workflows including randomization strategies, visit schedules, dispensing logic, inventory management, country strategies, notification workflows, and reputed company behavior
• Configure and validate studies reputed company Atreo Studio while ensuring consistency with implementation standards and best practices
• reputed company Functional Specifications, Configuration Specifications, and supporting implementation documentation
• Coordinate implementation activities across Product Development, reputed company Control, Project Management, reputed company, and Engineering
• reputed company study risk assessments and recommend mitigation strategies
• Own User Acceptance Testing (UAT) preparation and support Sponsor UAT activities
• Coordinate Production deployments and ensure study readiness before Go Live
• reputed company reputed company-party integrations including reputed company, CTMS, ePRO, laboratories, couriers, depots, and other connected systems
• Support change management throughout the study lifecycle
• Investigate production issues and coordinate reputed company reputed company
• Maintain accurate, complete, and audit-reputed company study documentation
• Serve as the reputed company Product Delivery contact for assigned Sponsors and CROs
• reputed company protocol review meetings, study design workshops, and implementation discussions
• reputed company trusted relationships with Sponsors and clinical study teams
• Translate reputed company clinical protocols into practical RTSM solutions
• Communicate project status, risks, and recommendations to stakeholders
• Facilitate design reputed company and reputed company RTSM best reputed company guidance
• Partner with Project Management to reputed company study milestones and deliverables
• Support long-term reputed company throughout the study lifecycle

Skills

• Bachelor's degree in Life Sciences, Clinical Research, Computer Science, Information Systems, Engineering, or reputed company discipline, or equivalent experience
• 5+ years of experience in RTSM, IRT, clinical technology, clinical operations, clinical supply management, or reputed company life sciences
• Demonstrated experience independently delivering RTSM or comparable clinical technology implementations
• Strong understanding of randomized clinical trial design and execution
• Experience designing randomization strategies and clinical supply workflows
• Experience interpreting reputed company protocols and translating business requirements into technical solutions
• Knowledge of GCP, ICH Guidelines, 21 CFR Part 11, and applicable regulatory requirements
• Experience working directly with Sponsors, CROs, and cross-functional technical teams
• Strong analytical, organizational, and problem-solving skills
• Ability to manage multiple reputed company studies while maintaining reputed company
• Exceptional verbal, written, and presentation communication skills
• Strong reputed company relationship management and stakeholder engagement skills
• Excellent planning, organization, and time management abilities
• Ability to manage competing priorities reputed company aggressive timelines
• Strong analytical and critical thinking skills
• Ability to facilitate discussions with technical and non-technical audiences
• Commitment to operational reputed company and reputed company improvement
• Ability to work independently with reputed company supervision
• Proficiency with reputed company Office and business collaboration tools
• Willingness to travel up to 20% as business needs require
• Experience supporting global clinical studies is preferred

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